Canonical Allele Identifier: CA362161432
Gene: NKX2-5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.172659897C>G (hg19) chr5:g.173232894C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173232894C>G , CM000667.2:g.173232894C>G GRCh38
NC_000005.9:g.172659897C>G , CM000667.1:g.172659897C>G GRCh37
NC_000005.8:g.172592503C>G NCBI36
NG_013340.1:g.7419G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000329198.5:c.650G>C MANE Select ENSP00000327758.4:p.Arg217Thr
ENST00000329198.4:c.650G>C ENSP00000327758.4:p.Arg217Thr
ENST00000424406.2:c.*603G>C ENSP00000395378.2:n.*603G>C
NM_001166175.1:c.*603G>C NP_001159647.1:n.*603G>C
NM_001166176.1:c.*449G>C NP_001159648.1:n.*449G>C
NM_004387.3:c.650G>C NP_004378.1:p.Arg217Thr
NM_004387.4:c.650G>C MANE Select NP_004378.1:p.Arg217Thr
NM_001166175.2:c.*603G>C NP_001159647.1:n.*603G>C
NM_001166176.2:c.*449G>C NP_001159648.1:n.*449G>C
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